Source: CLINVAR

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 85444
Gene Symbol: LRRCC1
LRRCC1
CUI: C0019209
Disease: Hepatomegaly
Hepatomegaly 		0.100 GeneticVariation CLINVAR

Entrez Id: 85444
Gene Symbol: LRRCC1
LRRCC1
CUI: C0022595
Disease: Keratosis Follicularis
Keratosis Follicularis 		0.100 GeneticVariation CLINVAR

Entrez Id: 85444
Gene Symbol: LRRCC1
LRRCC1
CUI: C0220726
Disease: Diastrophic dysplasia
Diastrophic dysplasia 		0.100 GeneticVariation CLINVAR

Entrez Id: 85444
Gene Symbol: LRRCC1
LRRCC1
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis 		0.100 GeneticVariation CLINVAR

Entrez Id: 85444
Gene Symbol: LRRCC1
LRRCC1
CUI: C0796074
Disease: MOHR-TRANEBJAERG SYNDROME
MOHR-TRANEBJAERG SYNDROME 		0.100 GeneticVariation CLINVAR

Entrez Id: 85444
Gene Symbol: LRRCC1
LRRCC1
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies 		0.100 GeneticVariation CLINVAR

Entrez Id: 85444
Gene Symbol: LRRCC1
LRRCC1
CUI: C3549567
Disease: Echogenic kidneys
Echogenic kidneys 		0.100 GeneticVariation CLINVAR

Entrez Id: 85444
Gene Symbol: LRRCC1
LRRCC1
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding) 		0.100 GeneticVariation CLINVAR